Next generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection.
MicroRNAs (miRNAs) are short, non-coding RNAs, which post-transcriptionally regulate gene expression and are proposed to play a key role in the regulation of innate and adaptive immunity. Here, we report a next generation sequencing (NGS) approach profiling the expression of miRNAs in primary bovine...
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2013
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oai:doaj.org-article:c2b8363d9ad4456cb795ff32942983e22021-11-18T07:54:57ZNext generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection.1932-620310.1371/journal.pone.0057543https://doaj.org/article/c2b8363d9ad4456cb795ff32942983e22013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23472090/?tool=EBIhttps://doaj.org/toc/1932-6203MicroRNAs (miRNAs) are short, non-coding RNAs, which post-transcriptionally regulate gene expression and are proposed to play a key role in the regulation of innate and adaptive immunity. Here, we report a next generation sequencing (NGS) approach profiling the expression of miRNAs in primary bovine mammary epithelial cells (BMEs) at 1, 2, 4 and 6 hours post-infection with Streptococcus uberis, a causative agent of bovine mastitis. Analysing over 450 million sequencing reads, we found that 20% of the approximately 1,300 currently known bovine miRNAs are expressed in unchallenged BMEs. We also identified the expression of more than 20 potentially novel bovine miRNAs. There is, however, a significant dynamic range in the expression of known miRNAs. The top 10 highly expressed miRNAs account for >80% of all aligned reads, with the remaining miRNAs showing much lower expression. Twenty-one miRNAs were identified as significantly differentially expressed post-infection with S. uberis. Several of these miRNAs have characterised roles in the immune systems of other species. This miRNA response to the Gram-positive S. uberis is markedly different, however, to lipopolysaccharide (LPS) induced miRNA expression. Of 145 miRNAs identified in the literature as being LPS responsive, only 9 were also differentially expressed in response to S. uberis. Computational analysis has also revealed that the predicted target genes of miRNAs, which are down-regulated in BMEs following S. uberis infection, are statistically enriched for roles in innate immunity. This suggests that miRNAs, which potentially act as central regulators of gene expression responses to a Gram-positive bacterial infection, may significantly regulate the sentinel capacity of mammary epithelial cells to mobilise the innate immune system.Nathan LawlessAmir B K ForoushaniMatthew S McCabeCliona O'FarrellyDavid J LynnPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 3, p e57543 (2013) |
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Medicine R Science Q Nathan Lawless Amir B K Foroushani Matthew S McCabe Cliona O'Farrelly David J Lynn Next generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection. |
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MicroRNAs (miRNAs) are short, non-coding RNAs, which post-transcriptionally regulate gene expression and are proposed to play a key role in the regulation of innate and adaptive immunity. Here, we report a next generation sequencing (NGS) approach profiling the expression of miRNAs in primary bovine mammary epithelial cells (BMEs) at 1, 2, 4 and 6 hours post-infection with Streptococcus uberis, a causative agent of bovine mastitis. Analysing over 450 million sequencing reads, we found that 20% of the approximately 1,300 currently known bovine miRNAs are expressed in unchallenged BMEs. We also identified the expression of more than 20 potentially novel bovine miRNAs. There is, however, a significant dynamic range in the expression of known miRNAs. The top 10 highly expressed miRNAs account for >80% of all aligned reads, with the remaining miRNAs showing much lower expression. Twenty-one miRNAs were identified as significantly differentially expressed post-infection with S. uberis. Several of these miRNAs have characterised roles in the immune systems of other species. This miRNA response to the Gram-positive S. uberis is markedly different, however, to lipopolysaccharide (LPS) induced miRNA expression. Of 145 miRNAs identified in the literature as being LPS responsive, only 9 were also differentially expressed in response to S. uberis. Computational analysis has also revealed that the predicted target genes of miRNAs, which are down-regulated in BMEs following S. uberis infection, are statistically enriched for roles in innate immunity. This suggests that miRNAs, which potentially act as central regulators of gene expression responses to a Gram-positive bacterial infection, may significantly regulate the sentinel capacity of mammary epithelial cells to mobilise the innate immune system. |
format |
article |
author |
Nathan Lawless Amir B K Foroushani Matthew S McCabe Cliona O'Farrelly David J Lynn |
author_facet |
Nathan Lawless Amir B K Foroushani Matthew S McCabe Cliona O'Farrelly David J Lynn |
author_sort |
Nathan Lawless |
title |
Next generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection. |
title_short |
Next generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection. |
title_full |
Next generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection. |
title_fullStr |
Next generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection. |
title_full_unstemmed |
Next generation sequencing reveals the expression of a unique miRNA profile in response to a gram-positive bacterial infection. |
title_sort |
next generation sequencing reveals the expression of a unique mirna profile in response to a gram-positive bacterial infection. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2013 |
url |
https://doaj.org/article/c2b8363d9ad4456cb795ff32942983e2 |
work_keys_str_mv |
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